Canonical Allele Identifier: CA409635468

Gene: CHRNA4

Linked Data

• dbSNP Id: rs142260793
• gnomAD v4: 20-63350378-G-T
• MyVariant Identifiers: chr20:g.61981730G>T (hg19) ; chr20:g.63350378G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350378G>T , CM000682.2:g.63350378G>T	GRCh38
NC_000020.10:g.61981730G>T , CM000682.1:g.61981730G>T	GRCh37
NC_000020.9:g.61452174G>T	NCBI36
NG_011931.1:g.15966C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.1033C>A MANE Select	ENSP00000359285.4:p.Arg345Ser
ENST00000370263.8:c.1033C>A	ENSP00000359285.4:p.Arg345Ser
ENST00000463705.5:n.1681C>A
ENST00000467563.3:n.1103C>A
ENST00000498043.6:c.1057C>A
ENST00000615287.4:c.820C>A	ENSP00000483388.1:p.Arg274Ser
ENST00000627000.1:c.*722C>A	ENSP00000486914.1:n.*722C>A
ENST00000630240.1:n.754C>A
NM_000744.6:c.1033C>A	NP_000735.1:p.Arg345Ser
NM_001256573.1:c.505C>A	NP_001243502.1:p.Arg169Ser
NR_046317.1:n.1289C>A
XM_011528524.1:c.820C>A	XP_011526826.1:p.Arg274Ser
XM_017027625.2:c.505C>A	XP_016883114.1:p.Arg169Ser
XM_024451822.1:c.505C>A	XP_024307590.1:p.Arg169Ser
NM_001256573.2:c.505C>A	NP_001243502.1:p.Arg169Ser
NR_046317.2:n.1242C>A
NM_000744.7:c.1033C>A MANE Select	NP_000735.1:p.Arg345Ser